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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 559860생성일: 2026년 10월 25일

2-Aminothiazole → 2-(3-Methoxy-2-methoxycarbonylphenoxy)-1-nitrobenzene

https://huagongshe.com/reaction/559860

반응식

참여 물질

역할이름HCID투입량
반응물2-AminothiazoleHCID 2155—
반응물1-Fluoro-2-nitrobenzeneHCID 73895—
반응물Methyl 2-hydroxy-6-methoxybenzoateHCID 527092—
반응물2-(3-Methoxy-2-methoxycarbonylphenoxy)anilineHCID 66998871—
생성물N-[(3-methoxy-2-methoxycarbonylphenoxy)phenyl]-N'-(thiazol-2-yl)ureaHCID 5973282165%
생성물2-(3-Methoxy-2-methoxycarbonylphenoxy)-1-nitrobenzeneHCID 6699883480%

반응 단계

2-(3-Methoxy-2-methoxycarbonylphenoxy)-1-nitrobenzene (1.21 g, 80%) was prepared from methyl 6-methoxysalicylate (1.09 g, 5.5 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This compound was reduced to 2-(3-methoxy-2-methoxycarbonylphenoxy)aniline (0.82 g, 75%) following the general procedure C. N-[(3-methoxy-2-methoxycarbonylphenoxy)phenyl]-N′-(thiazol-2-yl)urea (130 mg, 65%) was prepared from 2-(3-methoxy-2-methoxycarbonylphenoxy)aniline (136 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08063081B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-01945aeef199443792eeb6a08f2772a2
출처 메모uspto-grants-2011_11